Diafert for Embryo Selection and Fertility Improvement (DESTINy)
This trial is active, not recruiting.
|Treatments||daifert, control group|
|Start date||October 2015|
|End date||April 2017|
|Trial size||108 participants|
|Trial identifier||NCT02593513, 0040-103|
Prospective, single-center, single-blind, randomized, controlled, two-arm, interventional study.
|Endpoint classification||safety study|
|Intervention model||parallel assignment|
|Masking||single blind (subject)|
Percentage of successful implantations
time frame: At Week 6
Percentage of live births
time frame: Approximately Week 40 (pregnancy outcome)
Female participants at least 18 years old.
- Women at least 18 years old at the time of Informed Consent.
- Able to understand and voluntarily sign an Informed Consent form approved by the relevant Independent Ethics Committee (IEC) governing the site.
- First or second fresh Assisted Reproductive Technology (ART) cycle attempt (since last successful implantation, if any).
- Eligible for elective SET of fresh embryo on Day 2/3. Elective SET is defined as a transfer for which there is more than one embryo in the same morphological ("best") category as that of the selected embryo.
- Presence or history of ovarian endometriotic cyst.
- Presence or history of diagnosed severe endometriosis (i.e. stage IV of the revised American Fertility Society classification for endometriosis).
- Hormonal, functional, anatomical and/or other abnormalities potentially increasing the risk of miscarriage and/or ectopic pregnancy as judged by the Investigator and determined by medical history and clinical laboratory. This includes, but is not limited to, uncontrolled diabetes mellitus, uncontrolled thyroid disease, alcoholism, drug abuse, abnormal uterine cavity etc.
- History of two or more consecutive miscarriages.
- Known history of human immunodeficiency virus, Hepatitis C virus and/or Hepatitis B virus infection.
- The subject has other serious or acute conditions that, in the Investigator's opinion, would preclude her participation in the study.
- Need for preimplantation genetic diagnosis/screening.
- Use of time-lapse embryo imaging
- Participating in oocyte donation procedure.
- Participation in any interventional drug clinical investigation within 2 months prior to screening.
- Dependency on sponsor or investigator (e.g. co-worker or family member).
|Official title||A Prospective, Single-center, Randomized, Two-arm, Interventional Study to Evaluate the Implantation Rate of Embryos Selected on the Basis of Morphology and Granulocyte-Colony Stimulating Factor (G-CSF) Concentration in the Ovarian Follicular Fluid (FF) - FF G-CSF - Compared to the Implantation Rate of Embryos Selected on the Basis of Morphology Alone When Elective Single Embryo Transfer (SET) of a Fresh Embryo is Performed on Day 2/3 After Oocyte Retrieval|
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